Canonical Allele Identifier: CA996271476

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs1970354659
• gnomAD v3: 19-44949014-G-GTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCC
• gnomAD v4: 19-44949014-G-GTCCTCCCTCAGACCCAGGAGTCCAGGCCCCCAGCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949041_44949077dup , CM000681.2:g.44949041_44949077dup	GRCh38
NC_000019.9:g.45452298_45452334dup , CM000681.1:g.45452298_45452334dup	GRCh37
NC_000019.8:g.50144138_50144174dup	NCBI36
NG_008837.1:g.8056_8092dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.216-118_216-82dup (APOC2) MANE Select	ENSP00000252490.5:n.216-118_216-82dup
ENST00000252490.5:c.216-118_216-82dup (APOC4-APOC2)	ENSP00000252490.4:n.216-118_216-82dup
ENST00000585685.5:c.*999-118_*999-82dup (APOC4-APOC2)	ENSP00000467185.1:n.*999-118_*999-82dup
ENST00000585786.1:c.*177_*213dup (APOC2)	ENSP00000465001.1:n.*177_*213dup
ENST00000589057.5:c.447-118_447-82dup (APOC4-APOC2)	ENSP00000468139.1:n.447-118_447-82dup
ENST00000590360.2:c.216-118_216-82dup (APOC2)	ENSP00000466775.1:n.216-118_216-82dup
ENST00000591597.5:c.174-118_174-82dup (APOC2)	ENSP00000476835.1:n.174-118_174-82dup
ENST00000592257.5:c.*10-118_*10-82dup (APOC2)	ENSP00000477261.1:n.*10-118_*10-82dup
NM_000483.4:c.216-118_216-82dup (APOC2)	NP_000474.2:n.216-118_216-82dup
NR_037932.1:n.1423-118_1423-82dup (APOC4-APOC2)
NM_000483.5:c.216-118_216-82dup (APOC2) MANE Select	NP_000474.2:n.216-118_216-82dup